FDA NDC Directory · JSON-LD · Markdown

FULVESTRANT

NDC 70710-1688 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic namefulvestrant
Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA215234
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR
Active ingredientsFULVESTRANT (50 mg/mL)
Marketing started20211214
Package count1

External sources

Source: openFDA. Public-domain (CC0).